lisinopril and hydrochlorothiazide (68788-8224)

Drug Facts

Product Profile

Brand Name lisinopril and hydrochlorothiazide

Generic Name lisinopril and hydrochlorothiazide tablets

Labeler preferred pharmaceuticals inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 12.5 mg/1, lisinopril 10 mg/1

Manufacturer

Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8224

Product ID 68788-8224_08e4c28e-7c8d-4c00-81e0-bb56e2609765

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA076230

Listing Expiration 2026-12-31

Marketing Start 2022-09-12

Pharmacologic Class

Established (EPC)

thiazide diuretic [epc]

Chemical Structure

thiazides [cs]

Physiologic Effect

increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888224

Hyphenated Format 68788-8224

Supplemental Identifiers

RxCUI

197885

UNII

0J48LPH2TH E7199S1YWR

NUI

N0000175359 N0000175419 M0471776

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lisinopril and hydrochlorothiazide (source: ndc)

Generic Name lisinopril and hydrochlorothiazide tablets (source: ndc)

Application Number ANDA076230 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

12.5 mg/1
10 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (68788-8224-1)
30 TABLET in 1 BOTTLE (68788-8224-3)
60 TABLET in 1 BOTTLE (68788-8224-6)
90 TABLET in 1 BOTTLE (68788-8224-9)

source: ndc

Packages (4)

68788-8224-1 100 TABLET in 1 BOTTLE (68788-8224-1) 68788-8224-3 30 TABLET in 1 BOTTLE (68788-8224-3) 68788-8224-6 60 TABLET in 1 BOTTLE (68788-8224-6) 68788-8224-9 90 TABLET in 1 BOTTLE (68788-8224-9)

Ingredients (2)

hydrochlorothiazide (12.5 mg/1) lisinopril (10 mg/1)

Linked Drug Pages (1)

Lisinopril and Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "08e4c28e-7c8d-4c00-81e0-bb56e2609765", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197885"], "spl_set_id": ["9207c3bc-e12e-4017-8b85-0f928e744f64"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8224-1)", "package_ndc": "68788-8224-1", "marketing_start_date": "20220912"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8224-3)", "package_ndc": "68788-8224-3", "marketing_start_date": "20220912"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8224-6)", "package_ndc": "68788-8224-6", "marketing_start_date": "20220912"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8224-9)", "package_ndc": "68788-8224-9", "marketing_start_date": "20220912"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "68788-8224_08e4c28e-7c8d-4c00-81e0-bb56e2609765", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68788-8224", "generic_name": "Lisinopril and Hydrochlorothiazide Tablets", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LISINOPRIL", "strength": "10 mg/1"}], "application_number": "ANDA076230", "marketing_category": "ANDA", "marketing_start_date": "20220912", "listing_expiration_date": "20261231"}